l-carnitine for cyclic vomiting syndrome Response to treatment in 30 cases with Guidelines on management of cyclic
Description
Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia
doi: 10.1038/s41522-022-00266-3 67 PathakP.HelsleyR
L-carnitine is an amino acid
Physiol Behav 52:185187 Aureli T, Miccheli A, Ricciolini R, Di Cocco ME, Ramacci MT, Angelucci L, Ghirardi O, Conti F (1990) Aging brain: effect of acetyl-l-carnitine treatment on rat brain energy and phospholipid metabolism
